About the company
One of the major contributor of medicines globally ranking in top 10 pharma companies. The industry equipped with more than 1500 scientists with more than 5 million testing labs globally and over 36 clinical trials before the first perception. In the area of biotechnological medicine with 25000 clinical researchers testing every day world wide.
The company has located its head quarters in New York with the rank 57 in fortune 500 companies, founded in 1849, which is 170 years ago. Form have joint ventures with GSK and Mylan for improving the quality of medicines.
Large portfolio including branded and generics with products listed from A to Z. Applies rare diseases research to unveil the new therapy treatment, more than 30 million people in USA and 350 million globally uses the medicines for rare disease treatments. Several hematological and neurological rare disease therapies are in research phase. Gene therapy is one of the promising and rapidly developing portfolio in the companies profile, placing genetically corrected copies to patients cells. Having collaboration with Spark therapeutics investigating SPK-9001. As a snapshot 35 projects are in Phase 1, 34 are being in phase 2, 23 in phase 3, 9 went for registration with a total of 101 (metrics as of July 2019)
Constantly providing medicines in the areas of Hospital (anti infectives), oncology, anti inflammatory, oncology, rare diseases, biosimilars, vaccines and new molecular entities.
Partnering in social responsibility by delivering medicines in remote areas and uplifting the needed areas.
About the job
Experience for the job: 5-8 years
Qualification required for the job : Candidate need to have packaging development experience Especially in sterile injectables with regulatory knowledge in both generic and branded products And need to have a bachelors degree in science or engineering or a PG diploma in packaging technology
Candidate need to coordinate with external customer service suppliers and need to have Tarun knowledge on gap assessment technical data review discussions reviewing the bill of materials testing parameters review specifications packaging configurations and handling the technical documents labels barcodes artworks for the pre exhibit and exhibit batches
Candidate need to prepare and review the specifications for various packing materials
Candidate to require to coordinate with internal cross functional teams like analytical R&D quality control quality assurance regulatory firs productions engineering etc
Require to monitor the exhibit batches fielding visual inspection labelling and packing
Able to ensure the safety precautions and implement in the premises as per good laboratory practise and good manufacturing practises
Required to have knowledge on batch manufacturing reports and packaging records responsible for investigations related to the packing including stoppers filling oils visual inspection labelling issues